Strober Samuel
Division of Immunology and Rheumatology, Stanford University School of Medicine, CCSR Building, Room 2215-C, 269 Campus Drive, Stanford, CA, 94305-5166, USA,
Immunol Res. 2014 May;58(2-3):240-8. doi: 10.1007/s12026-014-8502-7.
Although organ and bone marrow transplantations are life-saving procedures for patients with terminal diseases, the requirement for the lifelong use of immunosuppressive drugs to prevent organ graft rejection and the development of graft versus host disease (GVHD) remain important problems. Experimental approaches to solve these problems, first in preclinical models and then in clinical studies, developed at Stanford during the past 40 years are summarized in this article. The approaches use fractionated radiation of the lymphoid tissues, a procedure initially developed to treat Hodgkin's disease, to alter the immune system such that tolerance to organ transplants can be achieved and GVHD can be prevented after the establishment of chimerism. In both instances, the desired goal was achieved when the balance of immune cells was changed to favor regulatory innate and adaptive immune cells that suppress the conventional immune cells that ordinarily promote inflammation and tissue injury.
尽管器官和骨髓移植对患有晚期疾病的患者来说是挽救生命的手术,但为防止器官移植排斥和移植物抗宿主病(GVHD)的发生而终身使用免疫抑制药物的需求仍然是重要问题。本文总结了过去40年在斯坦福大学首先在临床前模型中然后在临床研究中开发的解决这些问题的实验方法。这些方法使用最初为治疗霍奇金病而开发的对淋巴组织进行分次辐射的程序来改变免疫系统,以便在建立嵌合体后能够实现对器官移植的耐受并预防GVHD。在这两种情况下,当免疫细胞的平衡发生变化,有利于调节性固有免疫细胞和适应性免疫细胞,从而抑制通常促进炎症和组织损伤的传统免疫细胞时,就实现了预期目标。